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FDA 510(k)

ENDOTINE FOREHEAD DEVICE

K-Number: K032770 · 2003-10-08

Decision Date2003-10-08
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ENDOTINE FOREHEAD DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Coapt Systems, Inc.. It received FDA 510(k) clearance on 2003-10-08 under 510(k) number K032770. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOTINE FOREHEAD DEVICE?

ENDOTINE FOREHEAD DEVICE is a medical device that received FDA 510(k) clearance on 2003-10-08. The listed applicant is Coapt Systems, Inc.. The 510(k) number is K032770.

When did ENDOTINE FOREHEAD DEVICE receive FDA 510(k) clearance?

ENDOTINE FOREHEAD DEVICE received FDA 510(k) clearance on 2003-10-08, under 510(k) number K032770.

Who is the listed applicant for ENDOTINE FOREHEAD DEVICE?

The FDA 510(k) record lists Coapt Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOTINE FOREHEAD DEVICE?

The FDA product code for ENDOTINE FOREHEAD DEVICE is HWC. This falls under the Cardiovascular category.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Coapt Systems, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 17 devices →

Related Devices (Code: HWC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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